Remote Vinyasa Yoga Program for Heart Health
Feasibility, Acceptability, and Preliminary Efficacy of a Remote Vinyasa Yoga Program for Heart Health
1 other identifier
interventional
30
1 country
1
Brief Summary
The purpose of this study is to test a 12-week vinyasa yoga (flow yoga) intervention via Zoom. This program will be for 30 individuals with high blood pressure. 15 will receive the intervention and 15 will follow their usual routine. The investigators will determine if this vinyasa yoga program is feasible and acceptable in this population. Investigators will measure and compare blood pressure and other health responses such as physical health and well-being before and after participants complete the intervention or usual care period. The investigators hope to demonstrate that vinyasa yoga is a good option to improve heart health in people with high blood pressure. Primary Objective - Examine the feasibility, acceptability, and preliminary efficacy of a 12-wk remotely-delivered vinyasa yoga intervention (3 x per week) on cardiovascular (CV) health in adults with hypertension (HTN).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable hypertension
Started Aug 2025
Shorter than P25 for not_applicable hypertension
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 29, 2025
CompletedFirst Posted
Study publicly available on registry
May 8, 2025
CompletedStudy Start
First participant enrolled
August 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedAugust 17, 2025
April 1, 2025
9 months
April 29, 2025
August 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Carotid-Femoral Pulse Wave Velocity
Change from baseline to 12 weeks. Measure of central arterial stiffness (meters/second) measured by oscilometiric pulse wave velocity. A value of 10 m/s and above is classified as an unfavorable value.
Baseline to 12 weeks
Secondary Outcomes (29)
Change in systolic blood pressure
Baseline to 12 weeks
Change in diastolic blood pressure
Baseline to 12 weeks
Change in augmentation pressure
Baseline to 12 weeks
Change in augmentation index
Baseline to 12 weeks
Change in mean heart rate
Baseline to 12 weeks
- +24 more secondary outcomes
Study Arms (2)
Vinyasa Yoga
EXPERIMENTALParticipants will complete a 12-week, remotely-delivered intervention with three 60-minute vinyasa yoga sessions per week via Zoom, following an adapted Journey into Power yoga sequence by Baron Baptiste. The sessions will incorporate three mind-body components of yoga: through physical yoga poses, mindfulness, and breathing.
Standard Routine
NO INTERVENTIONStandard usual routine for 12 weeks
Interventions
Each yoga session will begin with 2 minutes of integration poses (Child's Pose, Downward Facing Dog, Ragdoll, and Mountain Pose), followed by \~20 minutes of Sun Salutations A and B (up to 5 of each). The Standing Series, lasting \~25 minutes, will include various standing and balancing poses from the Journey into Power sequence. Seated and supine stretches (including seated stretches, a yoga inversion, a reclined twist) will last \~8 minutes, and the session will conclude with 5 minutes of Savasana for final relaxation.
Eligibility Criteria
You may qualify if:
- Individuals with a resting systolic BP \>130 mmHg
You may not qualify if:
- Report currently meeting aerobic activity guidelines (150 min/wk)
- Practice yoga regularly (1 or more day/wk in the past month)
- Have physical limitations or a major medical condition contraindicating yoga or assessments
- Have uncontrolled HTN (systolic BP 160 mmHg or diastolic BP 100 mmHg)
- Are currently pregnant or planning to become pregnant within 6 months
- Are not on a stable dose of medications that could affect study outcomes
- Are concurrently enrolled in another lifestyle program
- No vulnerable populations will be included
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
West Virginia University
Morgantown, West Virginia, 26506, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Bethany Barone Gibbs, PhD
West Virginia University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
April 29, 2025
First Posted
May 8, 2025
Study Start
August 1, 2025
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
August 17, 2025
Record last verified: 2025-04